Classifications

• • G—PHYSICS
  • G01—MEASURING; TESTING
  • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
  • G01N1/00—Sampling; Preparing specimens for investigation
  • G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
  • G01N1/40—Concentrating samples
  • G01N1/4077—Concentrating samples by other techniques involving separation of suspended solids
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
  • B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
  • B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
  • B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
  • B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
  • B01L9/00—Supporting devices; Holding devices
  • B01L9/06—Test-tube stands; Test-tube holders
• • C—CHEMISTRY; METALLURGY
  • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
  • C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
  • C12M1/00—Apparatus for enzymology or microbiology
  • C12M1/26—Inoculator or sampler
• • C—CHEMISTRY; METALLURGY
  • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
  • C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
  • C12M33/00—Means for introduction, transport, positioning, extraction, harvesting, peeling or sampling of biological material in or from the apparatus
  • C12M33/04—Means for introduction, transport, positioning, extraction, harvesting, peeling or sampling of biological material in or from the apparatus by injection or suction, e.g. using pipettes, syringes, needles
• • C—CHEMISTRY; METALLURGY
  • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
  • C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
  • C12M47/00—Means for after-treatment of the produced biomass or of the fermentation or metabolic products, e.g. storage of biomass
  • C12M47/02—Separating microorganisms from the culture medium; Concentration of biomass
• • C—CHEMISTRY; METALLURGY
  • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
  • C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
  • C12M47/00—Means for after-treatment of the produced biomass or of the fermentation or metabolic products, e.g. storage of biomass
  • C12M47/04—Cell isolation or sorting
• • G—PHYSICS
  • G01—MEASURING; TESTING
  • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
  • G01N1/00—Sampling; Preparing specimens for investigation
  • G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
• • G—PHYSICS
  • G01—MEASURING; TESTING
  • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
  • G01N1/00—Sampling; Preparing specimens for investigation
  • G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
  • G01N1/40—Concentrating samples
• • G—PHYSICS
  • G01—MEASURING; TESTING
  • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
  • G01N1/00—Sampling; Preparing specimens for investigation
  • G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
  • G01N1/40—Concentrating samples
  • G01N1/405—Concentrating samples by adsorption or absorption
• • G—PHYSICS
  • G01—MEASURING; TESTING
  • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
  • G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
  • G01N35/10—Devices for transferring samples or any liquids to, in, or from, the analysis apparatus, e.g. suction devices, injection devices
• • G—PHYSICS
  • G01—MEASURING; TESTING
  • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
  • G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
  • G01N35/10—Devices for transferring samples or any liquids to, in, or from, the analysis apparatus, e.g. suction devices, injection devices
  • G01N35/1065—Multiple transfer devices
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
  • B01L2300/00—Additional constructional details
  • B01L2300/06—Auxiliary integrated devices, integrated components
  • B01L2300/0681—Filter
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
  • B01L2300/00—Additional constructional details
  • B01L2300/06—Auxiliary integrated devices, integrated components
  • B01L2300/069—Absorbents; Gels to retain a fluid
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
  • B01L2300/00—Additional constructional details
  • B01L2300/08—Geometry, shape and general structure
  • B01L2300/0832—Geometry, shape and general structure cylindrical, tube shaped
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
  • B01L2300/00—Additional constructional details
  • B01L2300/12—Specific details about materials
  • B01L2300/123—Flexible; Elastomeric
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
  • B01L2400/00—Moving or stopping fluids
  • B01L2400/04—Moving fluids with specific forces or mechanical means
  • B01L2400/0475—Moving fluids with specific forces or mechanical means specific mechanical means and fluid pressure
  • B01L2400/0478—Moving fluids with specific forces or mechanical means specific mechanical means and fluid pressure pistons
• • C—CHEMISTRY; METALLURGY
  • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
  • C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
  • C12M33/00—Means for introduction, transport, positioning, extraction, harvesting, peeling or sampling of biological material in or from the apparatus
  • C12M33/14—Means for introduction, transport, positioning, extraction, harvesting, peeling or sampling of biological material in or from the apparatus with filters, sieves or membranes
• • G—PHYSICS
  • G01—MEASURING; TESTING
  • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
  • G01N1/00—Sampling; Preparing specimens for investigation
  • G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
  • G01N1/2813—Producing thin layers of samples on a substrate, e.g. smearing, spinning-on
  • G01N2001/2826—Collecting by adsorption or absorption
• • G—PHYSICS
  • G01—MEASURING; TESTING
  • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
  • G01N1/00—Sampling; Preparing specimens for investigation
  • G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
  • G01N1/40—Concentrating samples
  • G01N1/4077—Concentrating samples by other techniques involving separation of suspended solids
  • G01N2001/4088—Concentrating samples by other techniques involving separation of suspended solids filtration

Definitions

• the invention relates to the field of the analysis of biological preparations for medical diagnostic purposes. More specifically, it relates to a device for capturing biological particles, in particular cells, in suspension in a liquid medium, and in particular in a biological sample.
• the invention also relates to a method for capturing such biological particles, as well as an apparatus for implementing this method.
• a device for the capture of biological particles is described in WO 2010/012941.
• This device comprises a tube closed by a filter membrane.
• An absorbent block is placed inside the tube.
• the absorption of water by the absorbent block makes it possible to control the flow entering the tube through the filtering membrane.
• Biological particles are then retained on the filter membrane.
• the filter membrane is then applied to a slide and an outflow is produced through the filter membrane to postpone a sample of cells, initially retained on the outer surface of the filter membrane, onto said slide.
• the cell layer reported on the slide advantageously makes it possible to perform a reliable cytological analysis.
• a cytological analysis makes it possible, in particular, to detect modifications that are at the origin or associated with diseases that may be life-threatening, in particular the detection of cancerous or precancerous conditions such as breast, urinary tract, uterine cancers, etc.
• Controlling the incoming flow through the filtering membrane makes it possible to retain a sufficient number of cells to obtain a cell sample that is statistically representative of the cell population in the liquid medium. It also avoids to obtain, on the filtering membrane, too many cells, which would lead to obtaining a cell sample in which the cells form clusters and / or stacks, that is to say say a sample from which the subsequent cytological analysis would not be optimal. In in particular, when the cells form clusters and / or stacks, there is a significant risk that cells of interest are inaccessible to cytological analysis.
• this object is achieved by means of a device for capturing biological particles suspended in a liquid medium, the device comprising:
• an absorbent block resting on the pad and able to absorb said liquid medium when in contact with said liquid medium, preferably able to swell under the effect of contact with said liquid medium, preferably hydrophilic; and a spring hindering the expansion and / or movement of the absorbent block away from the lower opening of the container, and in particular towards an upper end of the container, especially when the container is a said tube.
• the inventor has found that the interposition of such a buffer between the absorbent block and the filter membrane remarkably improves the homogeneity of the layer of biological particles retained on said filter membrane.
• the transfer of these biological particles on an analysis substrate, for example on a slide, advantageously leads to a more homogeneous sample, which leads to a more reliable analysis.
• the inventor explains this result by the capacity of the buffer foam to deform to compensate for the deformation of the absorbent block. This deformation thus does not substantially modify the distribution of the pressure exerted on the face of the buffer resting on the filter membrane, which remains uniform over the entire bearing area of the buffer on the filter membrane.
• a capture device preferably has one or more of the following optional features:
• the thickness of the buffer measured along the X axis, is greater than 1 mm and less than 4 mm;
• the buffer material is preferably polyurethane
• the buffer has a bottom face of complementary shape to the upper face of the filtering membrane
• the buffer is in contact with more than 80% of an upper face of the filtering membrane
• the device preferably comprises a stop impeding the movement of the spring away from the lower opening of the container, and in particular, when the container is a said tube, to the upper opening of the tube;
• the spring is a block of elastic foam
• the foam block is shaped so that, in a position in which it is housed inside the container, it is compressed by the side wall of the container
• the average pore size of the filtering membrane is greater than one micron and / or less than 25 microns, and / or the absorbent block consists of a hydrophilic material;
• the container is an X-axis tube opening, at lower and upper ends, through lower and upper openings, respectively;
• the difference between the largest transverse dimensions of the upper opening of the tube on the one hand and the buffer on the other hand is greater than 0.2 mm and less than 4 mm.
• the invention also relates to a method for capturing biological particles suspended in a liquid medium by means of a capture device according to the invention, said method comprising the following steps:
• step i) immersing the filter membrane of the container in the liquid medium, preferably while maintaining the upper end of said container; ii) holding the container in position (in the at least partially immersed position obtained at the end of step i)), in a stationary position or, preferably, oscillating about the X axis when the container is a said tube, in order to put the biological particles in homogeneous suspension within the liquid medium, for a sufficient time to retain on the filtering membrane particles contained in the flow of liquid medium entering the container and generated by the absorption of said liquid medium by the absorbent block;
• the invention also relates to an analysis apparatus comprising:
• the analysis apparatus comprises a finger holder, inserting fingers of the finger holder into containers of capture devices according to the invention respectively arranged on the support of containers, so as to constitute a rack of containers,
• An analysis apparatus preferably has one or more of the following optional features:
• each finger is preferably pierced with a light, said opening opening through upper and lower openings in fluid communication with the interior volume of a respective container, after constitution of the rack of containers, and with the internal volume of a bellows, respectively;
• the analysis apparatus comprising a jack configured to selectively press said bellows to increase the pressure within said container;
• each finger After constitution of the rack of containers, each finger has a lower end in contact with a spring of a said capture device.
• the invention also relates to a method for preparing a sample intended for a biological analysis, in particular a cyto logical analysis, said method comprising the following steps: a) obtaining at least one vial containing a liquid medium containing biological particles and, preferably, arranging said flask in a vial rack; b) preferably, independently of step a), provision of a capture device according to the invention on a container support;
• step b) when the analysis apparatus comprises at least one finger, introduction of said finger, preferably a finger of a finger-holder, through an upper opening of the container of the device, the finger being preferably shaped so that, in the position of maximum introduction of the finger into the container, the buffer contained in the container is in contact on the filter membrane fixed on said container;
• the preparation method can in particular be implemented by means of an analysis apparatus according to the invention. Definitions
• the capture device comprises a "container”
• the adjectives "upper” and “lower” are not limiting.
• the frame where the container is an X-axis tube they are defined with reference to a position of a device, in which the X-axis of the tube is substantially vertical (as in Figure 1).
• axial refers to the X axis of the tube.
• transverse means an orientation perpendicular to the X axis of the tube.
• biological particles is meant a particle that is not soluble in an aqueous liquid medium and that can be contained in a biological material taken from the body of a multicellular living organism, animal or plant, in particular an animal multicellular living organism, in particular a mammal, including the man.
• Tissue microfragments, micro-organisms, living cells, dead cells, anucleate cell bodies such as erythrocytes and platelets (thrombocytes), fragments, cell debris, as well as any crystals and light solid foreign bodies are examples of biological particles.
• Non-soluble protein substances such as pectin or fibronectin-derived protein substances, for example protein substances derived from fetal fibronectin, which represent a clinical parameter indicating a risk of preterm delivery, are other examples of particles.
• organic is an enzyme that causes a biological material taken from the body of a multicellular living organism, animal or plant, in particular an animal multicellular living organism, in particular a mammal, including the man.
• the “swelling capacity" of an absorbent block is the ratio between the volume of this block after maximum swelling by absorption of liquid medium and its initial dry volume.
• FIG. 1 represents an example of a capture device according to the invention, in a median longitudinal sectional plane
• FIG. 4 (4a-4i) schematically illustrates the different steps of a preparation method according to the invention, in one embodiment implementing an analysis apparatus according to the invention
• Figures 5 and 6 show second and third particular embodiments of a capture device according to the invention.
• FIG. 7 illustrates, schematically, an apparatus according to the invention.
• FIG. 1 represents a capture device 10 comprising a container in the form of an X-axis tube 12, a filter membrane 14, a buffer 16, an absorbent block 18 and a spring 20.
• the tube 12 has a cylindrical portion 22, preferably of circular cross section, terminated at the upper end of the tube 12, by a rim 24, preferably annular.
• the flange 24 is interrupted, thereby defining ears.
• the length of the tube is preferably greater than 5 cm and / or less than 10 cm.
• the largest transverse dimension of the cylindrical portion 22 is preferably greater than 1 cm and / or less than 4 cm.
• the thickness of the side wall defining the cylindrical portion 22 is preferably greater than 1 mm and / or less than 5 mm, preferably less than 3 mm.
• the tube 12 opens, at its upper and lower ends, through upper and lower openings, referenced 26s and 26i, respectively.
• the tube is made of plastic material, for example polyvinyl chloride, polystyrene or polyethylene.
• the tube 12 may comprise one or more of the characteristics of the tube referenced "101" described in WO 2010/012941.
• the tube may be of the type commonly used in automated biological sample processing systems for cytological analysis.
• Filter membrane
• the filter membrane 14 is fixed on the edge 28 of the tube 12 which defines the lower opening 26i, so as to completely close said lower opening.
• the filter membrane is glued, laser welded or heat sealed to said edge.
• filtering membranes known for cell filtration in the cytology field and in particular polyester or polycarbonate filtering membranes, for example the filtering membranes sold by MILLIPORE (BILLERICA, MA, USA) or by the company WHATAM GE HEALTHCARE (VERSAILLES, France), may be used.
• a filter membrane from IT4IP (Belgium) can also be used.
• the average pore size of the filter membrane is adapted to the intended application.
• the average pore size of the filter membrane is greater than one micron, greater than 3 ⁇ , or greater than 5 ⁇ , and / or less than 200 microns, less than 150 microns, less than 100 microns, less than 50. microns, or less than 25 microns.
• the filter membrane may be in particular the membrane referenced 7060-2511 sold by the company WHATAM GE HEALTHCARE.
• all of the biological particles of interest for cytological analysis can be taken by means of such a filtering membrane, whatever the nature or the tissue origin of the liquid medium.
• the filter membrane has an average pore size greater than 3 ⁇ , preferably greater than 5 ⁇ and / or less than 10 ⁇ , preferably less than 8 ⁇ , preferably less than 7 ⁇ .
• the filter membrane can then be in particular a filter membrane referenced TMTT-02500 sold by MILLIPORE or referenced TTT-B02500 marketed by MILLIPORE, or a Cyclopore® PC filter membrane such as 5 ⁇ membranes referenced 7060-2513 or 7060 -4713, 8 ⁇ , referenced 7060-2514 or 7060-4714 or 10 ⁇ , referenced 7060-2515 or 7060-4715.
• Such membranes can be in particular used to retain only large cells, for example of the type of epithelial cells resulting from a cervico-vaginal sample or smear.
• the buffer 16 also called “adapter buffer (TA)"
• TA adapter buffer
• the buffer 16 has an open porosity facilitating its passage through the liquid medium.
• the pad is configured so that its volume remains substantially constant when in contact with water, and more generally with the liquid having passed through the filtering membrane.
• the pad 16 has a lower face 16i of shape substantially complementary to the upper face 14s of the filter membrane 14.
• the faces 16i and 14s are substantially flat, preferably substantially transverse.
• the buffer 16 is in contact with more than 80%, preferably more than 90%, preferably more than 95%, preferably substantially 100% of the upper face 14s of the filter membrane 14 (exposed towards the inside of the tube 12).
• the pad 16 has a cylindrical shape of axis X.
• the lateral surface of the pad 16 is substantially complementary to the inner surface 121 of the tube 12.
• the pad has dimensions adapted so that it can to be moved freely in the tube. The assembly of the device is facilitated.
• the buffer introduced through the upper opening of the tube 12, can be slid, by gravity, along the tube, to abut with the filter membrane.
• the difference between the largest transverse dimensions of the upper opening of the tube on the one hand and the buffer on the other hand is greater than 0.2 mm, greater than 0.5 mm, preferably greater than 0, 8 mm and / or less than 4 mm, preferably less than 3 mm, preferably less than 2.5 mm.
• the thickness of the buffer, measured along the axis X is preferably constant, and preferably greater than 1 mm, preferably greater than 1.5 mm and / or preferably less than 4 mm, preferably less than 1 mm. 3 mm, preferably less than 2.5 mm. The best results were obtained with a thickness of 2 mm. Absorbent block
• Absorbent block 18 may have one or more of the characteristics of the block of absorbent material described in WO 2010/012941.
• the absorbent block 18 has a cylindrical shape of axis X, preferably of circular section, preferably substantially complementary to the inner surface 121 of the tube 12. Preferably, it has dimensions adapted so that it can be moved substantially freely inside the tube. The assembly of the device is facilitated.
• the absorbent block introduced through the upper opening of the tube 12, can thus be slid, by gravity, along the tube, to abut with the buffer 16.
• the difference between the largest transverse dimensions of the upper opening of the tube on the one hand and the absorbent block on the other hand is greater than 0.2 mm, greater than 0.5 mm, preferably greater than 0 , 8 mm and / or less than 4 mm, preferably less than 3 mm, preferably less than 2.5 mm.
• the thickness of the absorbent block, measured in the direction of the X axis, is preferably greater than 5 mm, greater than 8 mm, greater than 9 mm and / or less than 30 mm, less than 20 mm, preferably less than at 15 mm, preferably less than 12 mm.
• the absorbent block 18 has a lower face 18i of shape substantially complementary to the upper face 16s of the buffer 16.
• the faces 16s and 18i are substantially planar, preferably substantially transverse.
• Absorbent block 18 preferably comprises a material which swells upon contact with a liquid medium.
• the absorbent block is made of a hydrophilic material which swells when brought into contact with an aqueous liquid medium, in particular with water.
• this material preferably comprises viscose, preferably viscose compressed.
• the absorbent block 18 consists of a stack of viscose sheets, preferably non-woven viscose sheets, the stack of said sheets having been compressed. Viscose has the advantage of a good water absorption capacity, but also a good swelling capacity under the effect of this absorption.
• the absorbent block has a swelling capacity greater than 2, preferably greater than 3, preferably greater than 4.
• a swelling capacity can be obtained in particular with viscose.
• Absorbent block 18 may also comprise, or even consist of, a superabsorbent agent, well known to those skilled in the art, for example of the hydrogel type.
• the superabsorbent agent may in particular be a crosslinked sodium polyacrylate polymer, which may be obtained by a polymerization reaction of an acrylic acid mixed with sodium hydroxide in the presence of a polymerization initiator, a polyacrylamide copolymer, an ethylene maleic anhydride copolymer, a crosslinked carboxymethyl cellulose, a polyvinyl alcohol copolymer or a crosslinked polyethylene oxide.
• the swelling capacity is greater than 10, greater than 15, preferably greater than 20, or even greater than 30.
• Such a swelling capacity is possible in particular with crosslinked sodium polyacrylate, whose swelling capacity can to reach 60.
• the spring 20, or "spring buffer (TR)" has the function
• the elasticity of the spring is preferably sufficient to compensate for an elongation of the absorbent block, along the X axis, by more than 5%, preferably by more than 10% or even more than 15%.
• the spring 20 comprises a block of foam 30 disposed on the upper face 18s of the absorbent block 18.
• the foam block may have the shape of a rectangular parallelepiped, for example a cube, the largest dimension may be greater than 1 cm, greater than 1.5 cm, greater than 2 cm and / or less than 4 cm, or less than 3 cm.
• the elasticity of the foam block is preferably such that it makes it possible to reduce the volume by a factor greater than 2, preferably greater than 4, preferably greater than 6, preferably greater than 8, preferably greater than at 10, preferably greater than 15, preferably greater than 20, by manual compression, for example between the index finger and the thumb.
• the elasticity and the volume of the foam block are preferably determined so that the deformation of the foam block can elastically compensate for the increase in volume of the absorbent block during its swelling.
• the foam of the foam block 30 may be based on polyols and isocyanates. It can be made of polyurethane. It can be in particular RICHLUX HIGH RESILIENCE HR50065, RG50030 or RG50036, marketed by CARPENTER BELGIUM NV (Belgium).
• the foam block extends, inside the tube, over a height, measured along the axis X, of less than 4 cm, preferably less than 3 cm, preferably less than 2.5 cm. cm.
• the foam block is shaped so as to rub on the inner surface 121 of the side wall of the tube.
• the largest dimension in a cross-section of the foam block, measured while the foam block is out of the tube is slightly greater than the inside diameter of the tube, for example greater than 0.2 mm, greater than 0.5 mm, or greater than 1 mm diameter.
• the foam block To be introduced into the tube, the foam block must therefore be slightly compressed laterally.
• the need to compress laterally the foam block to introduce it into the tube facilitates the maintenance in the tube of the buffer 16 and the absorbent block 18.
• the friction of the foam block hampers its movement during the installation. expansion of the absorbent block.
• a stop is disposed above the foam block 30. This stop may be integrated in the device or be reported at the time where the device should be used, such as the finger described below.
• the foam block 30 has a lower face 30i substantially complementary to the upper face 18s of the absorbent block, preferably substantially planar, preferably substantially transverse.
• the shape of the foam block 30 is not limiting.
• the area of the lateral surface 301 of the foam block 30 which is in contact with the inner surface of the tube 12 is not limiting and can be advantageously modified depending on the desired spring effect.
• the spring 20 may also comprise or be constituted by other elastic means that a foam block, for example may comprise a helical spring whose lower end bears on the absorbent block 18 and the opposite end is immobilized by relative to the tube, at least temporarily, for example by a stop fixed on the tube.
• a foam block for example may comprise a helical spring whose lower end bears on the absorbent block 18 and the opposite end is immobilized by relative to the tube, at least temporarily, for example by a stop fixed on the tube.
• a capture device may advantageously be used with an analysis apparatus 48 according to the invention, illustrated in FIG. 7.
• An analysis apparatus 48 comprises a vial rack 50, a container rack, in this case a rack of tubes 52, constituted by assembling a container support, in this case a tube support 60, and an optional finger holder 70, optionally an analysis substrate rack 81 and a mechanism 55 for moving these different elements from each other to perform steps a) to f).
• the mechanism 55 of the analysis apparatus 48 is not limiting, provided that it allows the vial rack 50, the tube support 60, the finger holder 70 to be moved relative to one another, then the tube rack 52 resulting from the assembly of the tube support and the finger holder 70, and the rack of analysis substrates 81. The realization of such a mechanism does not pose any particular difficulties.
• an apparatus according to the invention further comprises an automaton 57 adapted to control the mechanism 55 so that the various process steps can be linked without human intervention.
• the vial rack 50 preferably has the form of a plate pierced with one or more orifices for a bottle 54 configured to each receive a vial 56 containing liquid medium loaded with biological particles to be captured.
• the vial rack 50 preferably has more than one, preferably more than two, preferably more than five, preferably more than ten vial ports 54 adapted to each retain a vial 56 in a substantially vertical position.
• the bottle 56 preferably has an annular flange which prevents it from passing through the bottle orifice 54 in which it is disposed.
• the tube rack 52 preferably comprises a tube support 60, preferably in the form of a plate pierced with one or more tube orifices 62 configured to each receive a capture device according to the invention.
• each tube orifice 62 may be shaped so as to allow the cylindrical portion 22 of the tube 12 to pass through a device, while preventing the passage of the rim 24.
• the number of tube ports 62 of the tube support 60 is preferably the same as the number of vial ports 54 of the vial rack.
• the tube rack 52 further comprises means for immobilizing each capture device on the tube support 60, for example jaws integral with the tube support and tightening the tubes suspended in their respective tube orifices.
• the finger holder 70 has one or more fingers 72 or “pushers” capable of being introduced into tubes arranged on the rack of tubes.
• each finger has, externally, the general shape of a substantially rectilinear rod.
• the length of a finger is preferably greater than 1 cm, 2 cm, 5 cm.
• the fingers project from a base 73, for example in the form of a plate, to which they are preferably rigidly fixed.
• the introduction of all the fingers into the respective tubes, in step c), can thus be advantageously simultaneous.
• the finger holder 70 has as many fingers as there are tube orifices 62 on the tube support 60. After introduction of a finger into a tube, as shown in FIG. 4c, the finger extends substantially along the axis X.
• each finger 72 is pierced with a longitudinal lumen 74 opening through lower openings 74i and 74s upper to the foam block 30 and in the interior of a bellows 76.
• the actuation of the bellows that is to say its compression so as to reduce the volume and allows to breathe the gas contained in the bellows, preferably air, within the longitudinal lumen 74, and therefore on the block of foam 30.
• the lower end of the finger is preferably in contact with the upper face 30s of the foam block 30, in a position which guarantees the pad is in contact with the filter membrane.
• the various components inside the tube have indeed been able to move, for example during their transport. If these components are no longer in the service position shown in Figure 1, the introduction of the finger pushes them towards the filter membrane until the foam block is in contact with the absorbent block, the absorbent block in contact with the buffer, and the pad in contact with the filter membrane ( Figure 1).
• the finger 72 may also serve as a stop to limit the movement of the foam block 30 towards the upper opening of the tube during the expansion of the absorbent block.
• the bellows 76 is provided with a vent 77 allowing limited air evacuation when pressure is exerted on the bellows 76 in order to reduce its volume. inside.
• the vent 77 also allows the inside of the tube 12 to be always at atmospheric pressure during the swelling of the absorbent block 18.
• the bellows which preferably has the shape of a nipple or a suction cup, is preferably fixed on the finger holder, and preferably on the upper surface of the finger holder 70, for example by means of rivets.
• Bottle 56 may in particular be a vial commonly used for the conditioning of cell or tissue samples for biological analysis purposes, including cyto logical or histological analyzes.
• the liquid medium 88 contained in the vial may consist of a buffered aqueous liquid medium containing a cell fixing agent or cell bodies in suspension.
• Fixing agents that may be mentioned include, for example, mixtures based on alcohol, for example the agent marketed under the SEDFIX® trademark by the company SURGIPATH or the product marketed under the trademark PRESERVCYT® by the company HOLOGIC or marketed under the brand name brand EASYFIX® by VWR.
• the liquid medium may consist of a saline buffer medium, preferably a suitable cell culture medium.
• the liquid medium may still consist of a natural body fluid such as blood, urine, or any natural or pathological physiological secretion such as ascites, effusion, cyst or flow.
• the tubes of a set of capture devices 10 according to the invention are arranged in the tube orifices 62 of a tube support 60, as illustrated in FIG. 4a.
• the capture devices are at least arranged in the tube orifices 62 which, when the tube rack and the vial rack are brought together, will face vials disposed in the vial orifices as shown in FIG. 4e.
• the fingers are arranged opposite the tube orifices 62 so as to be introduced into the tubes of the capture devices disposed in the tube orifices 62, as shown in FIG. 4b.
• the fingers 72 are then each introduced into a corresponding tube (FIG. 4b) until the finger holder 70 abuts the tube support 60.
• the assembly consisting of the tube support 60 and the finger holder 70 is a tube rack 52 which, preferably, is no longer separated until the end of the last step of the process ( Figure 4c).
• the tubes rack is arranged in such a way that the tubes that it carries are opposite the upper openings of the bottles 56 in order to be introduced into said bottles (FIG. 4e).
• the depth of penetration of the tubes into the flasks is determined so that the filtering membrane 14, the pad 16 and at least a portion of the filter block 18 of each tube are below the upper surface of the liquid medium contained in the flasks 56.
• the liquid medium thus penetrates inside the tube, through the filtering wall 14, then wets the absorbent block 18.
• the apparatus shown is intended for the simultaneous treatment of three sampling vials. The operation of the device is however the same regardless of the bottle considered. In the remainder of the description, this operation is therefore described for only one bottle.
• the filter block 18 contained in the tube introduced into this bottle absorbs a part of the liquid medium having penetrated into the tube 12 and inflates.
• the swelling of the absorbent block 18 leads to its expansion toward the upper opening of the tube, against the foam block 30, and towards the filtering membrane 14, against the pad 16 and the filtering membrane 14.
• the presence of the absorbent block ensures a minimum incoming flow, in particular by the surface tension force resulting from the surface energy characteristics of the absorbent block and the mechanical suction action resulting from the expansion of the absorbent block.
• the finger 72 opposes the movement of the foam block 30 towards the upper opening of the tube and therefore forces the latter to contract.
• the elasticity of the foam block 30 advantageously allows the absorbent block 18 to be held against the pad 16 and the pad 16 against the filter membrane 14.
• the buffer 16 allows a good distribution of the pressure exerted by the absorbent block 18 and ensures a substantially homogeneous incoming flow through the filtering membrane 14.
• the biological particles are retained on the lower face 14i of the filtering membrane 14.
• the uniformity of the flow of the liquid medium through the filtering membrane advantageously provides a homogeneous distribution of the biological particles on the underside 14i.
• the tube is kept in the flask for a determined period of time depending on the amount of biological particles to be fixed on the filtering membrane 14 (FIG. 4g).
• the holding in the partially submerged position preferably lasts more than 5 seconds and / or less than 10 minutes. Preferably, this duration is adapted to the nature of the liquid medium, and in particular to the concentration of the biological particles in the liquid medium, the desired density of biological particles on the filter membrane and the absorption capacity of the absorbent block.
• the tube rack is then removed from the vial rack, as shown in Figure 4h, so as to fully extract the tube from the vial.
• the biological particles are then recovered to form a sample adapted to be observed, in particular to perform a cytological analysis.
• the bottom surface 14i of the filter membrane is applied to an assay substrate 80, as shown in Fig. 4i.
• the tube is preferably kept out of the bottle and without contact with the analysis substrate for a waiting period of preferably greater than 5 seconds, preferably greater than 30 seconds, preferably greater than 1 minute, and preferably less than 5 minutes, preferably less than 3 minutes, preferably less than 2 minutes.
• This waiting period is preferably determined so that the absorbent block absorbs the residual liquid medium present in the tube and which is "free", that is to say which is not contained in the buffer or in the block. absorbent.
• the analysis substrate 80 may be in particular a slide.
• the analysis substrate 80 is disposed on a substrate rack 81, the substrate rack being preferably configured to receive as many test substrates as the tube support 60 can receive from tubes.
• the analysis apparatus comprises means for generating a flow of liquid medium exiting the tubes when the filtering membranes are applied to respective analysis substrates.
• a pressure is exerted on the bellows 76 (arrows in Figure 4i) to exert a pressure of a short duration.
• the deformation of the bellows is effected by means of an actuator 78 in the form of a jack whose rod is pressed quickly on said bellows.
• This overpressure creates a flow of liquid medium out of the tube, through the filter membrane 14, which leads to take off the biological particles of this membrane. The biological particles thus detached are thus transferred to the analysis substrate 80.
• the bellows elastically retakes its original shape.
• This method of transferring biological particles by replication of the filtering membrane is a method conventionally used by anatomopathologists.
• the filter membrane can be simply pressed against the analysis substrate.
• the sample may then be subjected to one or more treatment steps prior to its observation, for example one or more specific or nonspecific staining steps, including staining steps MAY-GR ⁇ MWALD GIESMA, staining known as "Papanicolaou”, staining Shorr, hematoxylin, eosin, etc.
• the transferred biological particles may also undergo an incubation step in the presence of detectable antibodies specific for membrane markers or intracellular markers, and / or treatment by a molecular biochemistry technique, for example by a technique of in situ hybridization with specific nucleic probes or a technique for extracting AR and quantifying the level of expression of one or more genes of interest, or a DNA extraction and mutation detection technique in the sequence of one or more genes of interest.
• a molecular biochemistry technique for example by a technique of in situ hybridization with specific nucleic probes or a technique for extracting AR and quantifying the level of expression of one or more genes of interest, or a DNA extraction and mutation detection technique in the sequence of one or more genes of interest.
• the filter membrane 14 is detached and the assembly constituted by the filter membrane and the biological particles retained are embedded in paraffin or a suitable resin, which is particularly useful for recovering tissue microfragments for of analysis, in particular for the realization of histological sections.
• the embodiment of the capture device illustrated in Figures 1 and 4 is particularly well suited for automation.
• the invention is however not limited to this embodiment.
• the capture device may comprise a piston 82, which replaces the finger 72 and the actuator 78. All steps can be performed manually, the piston being manually activated.
• the capture device advantageously comprises the means for manually separating the biological particles from the filtering membrane 14.
• the piston 82 may in particular comprise one or more of the optional characteristics of the piston "104" described in WO 2010/012941.
• the upper opening of the tube 12 may also be closed by a plug having an orifice guiding the sliding of the piston 82 in the tube.
• the piston is replaced by a bellows 84, similar to the bellows 76, and which operates identically.
• the bellows 84 is however fixed on the upper edge of the tube.
• a stop is provided to block the foam block 30.
• the shape of this stop is not limiting. It may for example be constituted by an inner tube 86 housed in the tube 12, similar to the finger 72, preferably immobilized relative to the tube. An upper rim 88 of the inner tube 86 may for example be sandwiched between the bellows 84 and the tube 12, as shown.
• the capture device is thus autonomous and can be used by hand.
• the invention provides a capture device that promotes, thanks to the presence of the buffer 16, a homogeneous particle distribution The reliability of the analyzes carried out on these biological particles is improved.
• the invention provides an analysis apparatus for automating the various steps of the method of preparing an observable sample, in particular for cytological analysis.
• This apparatus advantageously makes it possible to multiply the measurements made.
• the container is not limited to a tube. All the characteristics described above for a tube can therefore be applied to another form of container, except those which are specific to a tubular shape.
• the filter membrane is not necessarily attached to a lower end of the container, even if it is preferred.
• the container may have any dimensions and any structure, provided that it is shaped so that the spring hinders expansion and / or movement of the absorbent block.
• the spring can be integrated in the wall of the container, the wall of the container being preferably elastically deformable to hinder the expansion and / or movement of the absorbent block.
• the wall of the container may be constituted by an elastically deformable film and stretched so as to exert an elastic support on the absorbent block.
• the container does not have an upper opening.
• the container wall then defines with the filter membrane a closed chamber, preferably communicating with the outside only through the filter membrane.
• the wall of the container may be rigid or flexible.
• the invention is not limited to a particular field of application. For example, it can also be used to search for Legionnaires' disease.

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• 2016
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